Variant report

Variant	esv1824421
Chromosome Location	chr1:84704329-84719245
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:246)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:84713080-84713702	K562	blood:	n/a	n/a
2	ATF3	chr1:84712947-84713599	A549	lung:	n/a	n/a
3	ATF3	chr1:84712971-84713766	HCT-116	colon:	n/a	n/a
4	ATF3	chr1:84713134-84713579	K562	blood:	n/a	n/a
5	BCL3	chr1:84712879-84713635	A549	lung:	n/a	n/a
6	BCL3	chr1:84712912-84713611	A549	lung:	n/a	n/a
7	BHLHE40	chr1:84713184-84713547	K562	blood:	n/a	n/a
8	CBX3	chr1:84712907-84713811	HCT-116	colon:	n/a	n/a
9	CBX3	chr1:84712916-84713748	HCT-116	colon:	n/a	n/a
10	CCNT2	chr1:84711404-84711593	K562	blood:	n/a	n/a
11	CCNT2	chr1:84713360-84713562	K562	blood:	n/a	n/a
12	CEBPB	chr1:84713110-84713757	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr1:84712970-84713972	A549	lung:	n/a	n/a
14	CEBPB	chr1:84712526-84712776	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:84713298-84713479	K562	blood:	n/a	n/a
16	CEBPB	chr1:84716174-84716443	HepG2	liver:	n/a	chr1:84716354-84716367 chr1:84716301-84716318
17	CEBPB	chr1:84712503-84712775	A549	lung:	n/a	n/a
18	CEBPB	chr1:84716173-84716480	K562	blood:	n/a	chr1:84716354-84716367 chr1:84716301-84716318
19	CEBPB	chr1:84712408-84712879	A549	lung:	n/a	n/a
20	CEBPB	chr1:84713194-84713861	IMR90	lung:	n/a	n/a
21	CEBPB	chr1:84716152-84716456	A549	lung:	n/a	chr1:84716354-84716367 chr1:84716301-84716318
22	CEBPB	chr1:84713119-84713844	A549	lung:	n/a	n/a
23	CEBPB	chr1:84719191-84720434	HCT-116	colon:	n/a	n/a
24	CEBPB	chr1:84716166-84716424	IMR90	lung:	n/a	chr1:84716354-84716367 chr1:84716301-84716318
25	CEBPB	chr1:84713685-84713834	K562	blood:	n/a	n/a
26	CEBPD	chr1:84713288-84713673	K562	blood:	n/a	n/a
27	CEBPD	chr1:84713264-84713696	K562	blood:	n/a	n/a
28	CHD1	chr1:84712968-84713901	IMR90	lung:	n/a	n/a
29	CHD2	chr1:84713269-84713513	Hela-S3	cervix:	n/a	n/a
30	CREB1	chr1:84713192-84713612	A549	lung:	n/a	n/a
31	CREB1	chr1:84713035-84713385	A549	lung:	n/a	n/a
32	CREB1	chr1:84713174-84713510	GM12878	blood:	n/a	n/a
33	CTCF	chr1:84711171-84711209	Pancreas_OC	pancreas:	n/a	n/a
34	CTCF	chr1:84711076-84711320	GM12878	blood:	n/a	n/a
35	CTCF	chr1:84713360-84713510	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr1:84711100-84711250	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr1:84717020-84717170	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr1:84713240-84713390	HCT-116	colon:	n/a	n/a
39	CTCF	chr1:84711195-84711253	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr1:84711158-84711313	HUVEC	blood vessel:	n/a	n/a
41	E2F4	chr1:84712701-84713432	MCF10A-Er-Src	breast:	n/a	n/a
42	EP300	chr1:84713157-84713601	K562	blood:	n/a	n/a
43	EP300	chr1:84713027-84713750	SK-N-SH	brain:	n/a	n/a
44	EP300	chr1:84713175-84713372	GM12878	blood:	n/a	n/a
45	EP300	chr1:84712891-84713798	A549	lung:	n/a	n/a
46	EP300	chr1:84712878-84713823	A549	lung:	n/a	n/a
47	EP300	chr1:84713054-84713547	Hela-S3	cervix:	n/a	n/a
48	FOS	chr1:84711343-84711686	HUVEC	blood vessel:	n/a	n/a
49	FOS	chr1:84713021-84713624	MCF10A-Er-Src	breast:	n/a	chr1:84713230-84713241
50	FOS	chr1:84712952-84713629	HUVEC	blood vessel:	n/a	chr1:84713230-84713241

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:84709527-84709577	HMEC	breast:	n/a
2	chr1:84709527-84709577	IMR90	lung:	fetal
3	chr1:84709527-84709577	Caco-2	colon:	n/a
4	chr1:84709527-84709577	LNCaP	prostate:	n/a
5	chr1:84709527-84709577	HRCEpiC	kidney:	n/a
6	chr1:84709527-84709577	HRE	kidney:	n/a
7	chr1:84709527-84709577	SK-N-SH_RA	brain:	n/a
8	chr1:84709527-84709577	Jurkat	blood:	n/a
9	chr1:84709527-84709577	A549	lung:	n/a
10	chr1:84709527-84709577	Hepatocyte	liver:	n/a
11	chr1:84709527-84709577	GM12878	blood:	n/a
12	chr1:84709527-84709577	K562	blood:	n/a
13	chr1:84709527-84709577	HCT-116	colon:	n/a
14	chr1:84709527-84709577	HL-60	blood:	n/a
15	chr1:84709527-84709577	HIPEpiC	eye:	n/a
16	chr1:84709527-84709577	SAEC	small airway:	n/a
17	chr1:84709527-84709577	HepG2	liver:	n/a
18	chr1:84709527-84709577	GM06990	blood:	n/a
19	chr1:84709527-84709577	RPTEC	kidney:	n/a
20	chr1:84709527-84709577	T-47D	breast:	n/a
21	chr1:84709527-84709577	HPAEpiC	pulmonary alveolar:	n/a
22	chr1:84709527-84709577	AoSMC	blood vessel:	n/a
23	chr1:84709527-84709577	PANC-1	pancreas:	n/a
24	chr1:84709527-84709577	NB4	blood:	n/a
25	chr1:84709527-84709577	HCM	heart:	n/a
26	chr1:84709527-84709577	MCF-7	breast:	n/a
27	chr1:84709527-84709577	AG09319	gingival:	n/a
28	chr1:84709527-84709577	SKMC	muscle:	n/a
29	chr1:84709527-84709577	HNPCEpiC	eye:	n/a
30	chr1:84709527-84709577	NHBE	bronchial:	n/a
31	chr1:84709527-84709577	HAEpiC	amniotic membrane:	n/a
32	chr1:84709527-84709577	PFSK-1	brain:	n/a
33	chr1:84709527-84709577	BE2_C	brain:	n/a
34	chr1:84709527-84709577	NT2-D1	testis:	n/a
35	chr1:84709527-84709577	HCPEpiC	choroid plexus:	n/a
36	chr1:84709527-84709577	HEK293	kidney:	embryo
37	chr1:84709527-84709577	Hela-S3	cervix:	n/a
38	chr1:84709527-84709577	HRPEpiC	eye:	n/a
39	chr1:84709527-84709577	ECC-1	luminal epithelium:	n/a
40	chr1:84709527-84709577	NHDF-neo	bronchial:	n/a
41	chr1:84709527-84709577	PrEC	prostate:	n/a
42	chr1:84709527-84709577	HEEpiC	esophagus:	n/a
43	chr1:84709527-84709577	NH-A	brain:	n/a
44	chr1:84709527-84709577	AG04449	skin:	fetal
45	chr1:84709527-84709577	GM12892	blood:	n/a
46	chr1:84709527-84709577	SK-N-SH	brain:	n/a
47	chr1:84709527-84709577	U87	brain:	n/a
48	chr1:84709527-84709577	H1-hESC	embryonic stem cell:	embryo
49	chr1:84709527-84709577	GM19239	blood:	n/a
50	chr1:84709527-84709577	HUVEC	blood vessel:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:84708889..84710683-chr1:84712706..84714926,2	MCF-7	breast:
2	chr1:84703877..84705548-chr1:84707085..84709584,2	K562	blood:
3	chr1:84703877..84705548-chr1:84707085..84709584,2	K562	blood:
4	chr1:84707348..84709881-chr1:84716416..84718748,2	K562	blood:
5	chr1:84717533..84719612-chr1:84721999..84724485,2	K562	blood:
6	chr1:84719167..84721681-chr1:84724768..84726729,2	MCF-7	breast:
7	chr1:84707348..84709881-chr1:84716416..84718748,2	K562	blood:
8	chr1:84718460..84721280-chr1:84722520..84725212,2	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKACB-5	chr1:84710017-84710260	NONHSAT004193

No data

Variant related genes	Relation type
ENSG00000226970	TF binding region
ENSG00000226970	CpG island
ENSG00000226970	chromatin interactions

Extended variants
information (count: 591 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:591 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13375357	chr1:84704329-84704330	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187986175	chr1:84704330-84704331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536326084	chr1:84704335-84704336	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs41301216	chr1:84704355-84704356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567319561	chr1:84704421-84704422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574582581	chr1:84704461-84704462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536584110	chr1:84704490-84704491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546569141	chr1:84704533-84704534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566113488	chr1:84704582-84704583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534701227	chr1:84704665-84704666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557692050	chr1:84704673-84704674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374281119	chr1:84704690-84704691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577733305	chr1:84704720-84704721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs41301218	chr1:84704744-84704745	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs557562340	chr1:84704745-84704746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556287240	chr1:84704769-84704770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574134367	chr1:84704805-84704806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs193095065	chr1:84704823-84704824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559789970	chr1:84704846-84704847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs41301220	chr1:84704937-84704938	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs545030888	chr1:84704944-84704945	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564833281	chr1:84704960-84704961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530645128	chr1:84704969-84704970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550381735	chr1:84705225-84705226	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs41301222	chr1:84705233-84705234	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs113134055	chr1:84705266-84705267	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs529846162	chr1:84705350-84705351	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs576018749	chr1:84705362-84705363	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs546729107	chr1:84705371-84705372	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs545083133	chr1:84705382-84705383	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs576712742	chr1:84705400-84705401	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs538512406	chr1:84705417-84705418	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs72940018	chr1:84705418-84705419	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs548001913	chr1:84705439-84705440	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs576655359	chr1:84705440-84705441	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs371095224	chr1:84705450-84705451	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs577874735	chr1:84705452-84705453	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs571288235	chr1:84705453-84705454	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs537583674	chr1:84705457-84705458	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs787858	chr1:84705481-84705482	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs11163925	chr1:84705494-84705495	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs536448575	chr1:84705504-84705505	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs553490553	chr1:84705529-84705530	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs573592583	chr1:84705572-84705573	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs386633027	chr1:84705585-84705586	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs41301224	chr1:84705586-84705587	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs35348281	chr1:84705608-84705609	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs535822738	chr1:84705611-84705612	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs41301226	chr1:84705617-84705618	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs188821595	chr1:84705634-84705635	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84657600-84708000	Weak transcription	Left Ventricle	heart
2	chr1:84666800-84710200	Weak transcription	HSMMtube	muscle
3	chr1:84672600-84711200	Weak transcription	Brain Substantia Nigra	brain
4	chr1:84675200-84712800	Weak transcription	NH-A	brain
5	chr1:84675800-84705000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:84685400-84705400	Weak transcription	HUVEC	blood vessel
7	chr1:84685400-84705600	Weak transcription	Brain Germinal Matrix	brain
8	chr1:84685600-84713400	Weak transcription	Rectal Smooth Muscle	rectum
9	chr1:84690000-84719400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr1:84690200-84707400	Weak transcription	Right Ventricle	heart
11	chr1:84690400-84705000	Weak transcription	Aorta	Aorta
12	chr1:84690400-84711800	Weak transcription	Spleen	Spleen
13	chr1:84691200-84712200	Weak transcription	Pancreas	Pancrea
14	chr1:84691400-84705000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr1:84691400-84707000	Weak transcription	Fetal Stomach	stomach
16	chr1:84691600-84705000	Weak transcription	Fetal Muscle Trunk	muscle
17	chr1:84697400-84705000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr1:84698600-84705400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr1:84699000-84707000	Weak transcription	Psoas Muscle	Psoas
20	chr1:84699600-84713000	Weak transcription	Duodenum Mucosa	Duodenum
21	chr1:84699800-84711600	Weak transcription	A549	lung
22	chr1:84700400-84706200	Strong transcription	Primary T helper cells fromperipheralblood	blood
23	chr1:84700600-84705800	Strong transcription	Primary T cells fromperipheralblood	blood
24	chr1:84700600-84705800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr1:84700600-84705800	Strong transcription	Brain Hippocampus Middle	brain
26	chr1:84700600-84706000	Strong transcription	Primary B cells from peripheral blood	blood
27	chr1:84700600-84706200	Strong transcription	Fetal Thymus	thymus
28	chr1:84700600-84706200	Strong transcription	Dnd41	blood
29	chr1:84700600-84706600	Strong transcription	Primary T cells from cord blood	blood
30	chr1:84700600-84706600	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr1:84700800-84705600	Strong transcription	Primary T helper cells PMA-I stimulated	--
32	chr1:84700800-84706200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr1:84701200-84705400	Strong transcription	Primary hematopoietic stem cells	blood
34	chr1:84701200-84705600	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr1:84701200-84706000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr1:84701200-84707000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:84701200-84707000	Weak transcription	Colon Smooth Muscle	Colon
38	chr1:84701200-84707200	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr1:84701200-84707600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr1:84701200-84711800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr1:84701200-84713200	Weak transcription	Colonic Mucosa	Colon
42	chr1:84701200-84717400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr1:84701200-84718400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr1:84701200-84719600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr1:84701400-84705000	Weak transcription	Brain Angular Gyrus	brain
46	chr1:84701400-84705000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr1:84701400-84705000	Weak transcription	Fetal Brain Female	brain
48	chr1:84701400-84705200	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr1:84701400-84705400	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr1:84701400-84705400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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